The following data is part of a premarket notification filed by Jeil Medical Corporation with the FDA for Arix Hand System.
Device ID | K161746 |
510k Number | K161746 |
Device Name: | ARIX Hand System |
Classification | Plate, Fixation, Bone |
Applicant | Jeil Medical Corporation Seoul, KR 152-728 |
Contact | Seungyong Lee |
Correspondent | Seungyong Lee Jeil Medical Corporation Seoul, KR 152-728 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-06-24 |
Decision Date | 2016-09-21 |
Summary: | summary |